Canonical Allele Identifier: PA294499
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 135839
ClinVar RCV Id: RCV000132157 RCV000408980 RCV001030498 RCV001257068 RCV001355067 RCV003492535 RCV000588824 RCV004528840 RCV001796965
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1051Ile
CA011639
NM_000179.3:c.3151G>A